Overview of IMPROWISE
A comprehensive platform for managing all your clinical trial activities including CTPM, CDMS, CTBM, eTMF, ePRO, RBACS, and audit monitoring; securely and cost-effectively.
A CTMS is responsible for managing all operational aspects of a clinical trial, from study startup to closeout. CTMS serves as a central information hub for study stakeholders to effectively plan, implement, manage, and analyze their entire clinical study portfolio.
While CDMS is responsible for collecting, cleansing, and maintaining accurate, high-quality data compliant with all regulations. The key function of CDMS is to reduce errors in data handling and make it qualified for analysis in minimum cycle time.
Clinical trials are extremely complex. Biotech, pharmaceuticals, and other research-focused life sciences organizations run highly complicated clinical trials in the search for new medicines, devices, and the ultimate cure for many of the world’s diseases. Using software helps you manage clinical trials in clinical research.
IMPROWISE platform is an easy-to-use clinical trial management system and clinical data management system that helps clinical operations teams accelerate timelines, stay organized, and reduce complexity.
If you are interested in learning more, you can schedule a free demo.
ImproWise is a comprehensive Clinical Trial Management and Data Management Platform engineered to seamlessly manage multiple trials through a single user login.
The array of features within ImproWise collaboratively streamline, enhance efficiency, and fortify the security of clinical trial management, ultimately elevating the success rate and compliance of clinical trials.
The array of features within ImproWise collaboratively streamline, enhance efficiency, and fortify the security of clinical trial management, ultimately elevating the success rate and compliance of clinical trials.
Using “ImproWise”, eCRFs can be designed very quickly; CDB developed simultaneously, and DB annotation & validation done simultaneously. This reduces the time involved, resources, and cost appreciably.
Following the methodology SAAS (Software as a Service); Sponsors, Principal Investigators, Project Managers, Finance Heads, and other stakeholders can assign a certain cost to their project and forget about overloading their budget. “ImproWise” brings you appreciable cost, time, and resource savings. It is HIPAA and 21CFR compliant.
Since “ImproWise” is Web and cloud-based, tracking of the currently configured Clinical Trial / Study is possible via the Dynamic Dashboards designed for the authorized users/decision makers.
- Provides an unparalleled data infrastructure, seamless connectivity, and intuitive design to drive smarter, faster trials with a configurable, scalable, SaaS-based solution
- Supports the needs of emerging Pharma, BioPharma, and Device manufacturers, through global mega-trials in one integrated application built on a health-cloud platform
- Configures quickly using pre-built connectors and templates
- Intuitively tracks and logically structures information to enable life science teams to monitor and report on clinical trial progress and make better-informed decisions, providing the best quality data while ensuring subject safety
- Uses AI and ML and is engineered for flexible business models
- Recommends the next-best action using built-in predictive intelligence
- Ensures your clinical processes, security, and compliance with regulatory guidelines are always current with several annual upgrades
ImproWise Enhances The Clinical Trial Process.
Improwise offers a comprehensive and adaptable Clinical Trial Management System (CTMS) that consolidates all essential components. Pioneering the industry, it is the first on-demand, subscription-based CTMS. It includes CTPM, CDMS, CTBM, eTMF, ePRO, RBACS, and Audit Monitoring modules. As per requirement modules will be assigned to study which optimizes the cost.
Benefits of ImproWise
Module-Based Access
Choose and utilize only the necessary modules such as CDM, Monitoring (Study Audit), Patient Diary, and Study Finance, optimizing costs.
Flexible Pricing
Pricing adapts to the complexity of each trial, ensuring cost-effectiveness.
License-Based Model
The platform is licensed per trial with no perpetual costs, providing financial flexibility.
Reduced Training Time
Minimal training requirements lead to faster system deployment and reduced training costs.
Centralized Control
Manage multiple locations from a single platform, lowering project management costs and operational expenses.
Cost Savings on Regulatory Approvals
Electronic data format and full compliance reduce expenses related to regulatory approvals.
Efficient Data Submission
Quickly fulfill additional regulatory data submission demands, controlling overhead costs.
Minimal IT CapEx
Low capital expenditure on IT hardware, reducing initial setup costs.
Faster Time-to-Market for Drugs and Therapies
Accelerates trial workflows, and expedites data analysis and regulatory submission.
Capabilities of ImproWise
- Secure Web-Based Access: Accessible from anywhere and at any time through a secure web interface, ensuring data privacy and convenience.
- 100% Mobile Friendly and responsive: Improwise is adaptable to different screen resolutions and different devices and is fully mobile-friendly. Hence, there is no need to have a native App on your mobile.
- Dynamic eCRF Design: Ability to design electronic Case Report Forms (eCRFs) dynamically on the fly, often within a few days, a unique and time-saving feature.
- Efficient eCRF Development: Simultaneous design, annotation, and validation of eCRFs and Clinical Data Banks (CDBs) in a matter of days, resulting in significant cost savings.
- Multi-Trial, Multi-Site Handling: Capable of managing multiple trials and multiple sites within a single system and through a single login simultaneously, streamlining trial management.
- Dynamic, Database-Driven System: A highly adaptable system driven by a database, requiring minimal customization for different trials.
- Easy Field Customization: Ability to add new fields to accommodate trial-specific requirements with minimal programming effort.
- User-Friendly Query Builder: A highly flexible query builder accessible to non-technical staff, including Clinical Research Coordinators (CRC), doctors, and Principal Investigators, without the need for programming knowledge.
- Real-Time Trial Tracking: Real-time tracking of ongoing trials, allowing for timely monitoring and decision-making.
- HIPAA Compliance: Ensures compliance with the Health Insurance Portability and Accountability Act (HIPAA) standards for data security and privacy.
- Customized Reporting: Tailored reporting capabilities to meet the specific needs of each clinical trial.
- Management Dashboard: Offers multiple dashboards to access key insights and monitor trial progress, highlighting each milestone and the current status of the study.
- Comprehensive Audit Trail: Audit trailing for every data element entered and changed by CRCs, Quality Assurance (QA) personnel, or Principal Investigators, ensuring data integrity and accountability.
